Risultati della ricerca - Lambert, Christophe G

Search for compound heterozygous effects in exome sequence of unrelated subjects di Christensen, G Bryce, Lambert, Christophe G

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Learning from our GWAS mistakes: from experimental design to scientific method di Lambert, Christophe G., Black, Laura J.

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Genome-Wide Association Study in Bipolar Patients Stratified by Co-Morbidity di Kerner, Berit, Lambert, Christophe G., Muthén, Bengt O.

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Bipolar disorder and diabetes mellitus: evidence for disease-modifying effects and treatment implications di Charles, Ellen F., Lambert, Christophe G., Kerner, Berit

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LocalControl: An R Package for Comparative Safety and Effectiveness Research di Lauve, Nicolas R., Nelson, Stuart J., Young, S. Stanley, Obenchain, Robert L., Lambert, Christophe G.

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Imputation and characterization of uncoded self-harm in major mental illness using machine learning di Kumar, Praveen, Nestsiarovich, Anastasiya, Nelson, Stuart J, Kerner, Berit, Perkins, Douglas J, Lambert, Christophe G

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Molecular basis of reduced LAIR1 expression in childhood severe malarial anaemia: Implications for leukocyte inhibitory signalling di Achieng, Angela O., Guyah, Bernard, Cheng, Qiuying, Ong'echa, John M., Ouma, Collins, Lambert, Christophe G., Perkins, Douglas J.

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Ingestion of hemozoin by peripheral blood mononuclear cells alters temporal gene expression of ubiquitination processes di Anyona, Samuel B., Cheng, Qiuying, Raballah, Evans, Hurwitz, Ivy, Lambert, Christophe G., McMahon, Benjamin H., Ouma, Collins, Perkins, Douglas J.

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Comprehensive comparison of monotherapies for psychiatric hospitalization risk in bipolar disorders di Nestsiarovich, Anastasiya, Mazurie, Aurélien J, Hurwitz, Nathaniel G, Kerner, Berit, Nelson, Stuart J, Crisanti, Annette S, Tohen, Mauricio, Krall, Ronald L, Perkins, Douglas J, Lambert, Christophe G

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Hypothyroidism risk compared among nine common bipolar disorder therapies in a large US cohort di Lambert, Christophe G, Mazurie, Aurélien J, Lauve, Nicolas R, Hurwitz, Nathaniel G, Young, S Stanley, Obenchain, Robert L, Hengartner, Nicolas W, Perkins, Douglas J, Tohen, Mauricio, Kerner, Berit

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Trends in Patient Procurement of Postoperative Opioids and Route of Hysterectomy in the United States from 2004 to 2014 di THOMPSON, Jennifer C., KOMESU, Yuko M., QEADAN, Fares, JEPPSON, Peter C., CICHOWSKI, Sara C., ROGERS, Rebecca G., MAZURIE, Aurélien J., NESTSIAROVICH, Anastasiya, LAMBERT, Christophe G., DUNIVAN, Gena C.

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Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf–Hirschhorn syndrome di Ho, Karen S, South, Sarah T, Lortz, Amanda, Hensel, Charles H, Sdano, Mallory R, Vanzo, Rena J, Martin, Megan M, Peiffer, Andreas, Lambert, Christophe G, Calhoun, Amy, Carey, John C, Battaglia, Agatino

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Genetic variation in interleukin-7 is associated with a reduced erythropoietic response in Kenyan children infected with Plasmodium falciparum di Kisia, Lily E., Kempaiah, Prakasha, Anyona, Samuel B., Munde, Elly O., Achieng, Angela O., Ong’echa, John M., Lambert, Christophe G., Chelimo, Kiprotich, Ouma, Collins, Perkins , Douglas J., Raballah, Evans

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Cyclooxygenase-2 haplotypes influence the longitudinal risk of malaria and severe malarial anemia in Kenyan children from a holoendemic transmission region di Anyona, Samuel B., Hengartner, Nicolas W., Raballah, Evans, Ong’echa, John Michael, Lauve, Nick, Cheng, Qiuying, Fenimore, Paul W., Ouma, Collins, Lambert, Christophe G., McMahon, Benjamin H., Perkins, Douglas J.

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Differential Gene Expression in Host Ubiquitination Processes in Childhood Malarial Anemia di Anyona, Samuel B., Raballah, Evans, Cheng, Qiuying, Hurwitz, Ivy, Ndege, Caroline, Munde, Elly, Otieno, Walter, Seidenberg, Philip D., Schneider, Kristan A., Lambert, Christophe G., McMahon, Benjamin H., Ouma, Collins, Perkins, Douglas J.

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Integrated OMICS platforms identify LAIR1 genetic variants as novel predictors of cross-sectional and longitudinal susceptibility to severe malaria and all-cause mortality in Kenya... di Achieng, Angela O., Hengartner, Nicolas W., Raballah, Evans, Cheng, Qiuying, Anyona, Samuel B., Lauve, Nick, Guyah, Bernard, Foo-Hurwitz, Ivy, Ong'echa, John M., McMahon, Benjamin H., Ouma, Collins, Lambert, Christophe G., Perkins, Douglas J.

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Identification of Rare Recurrent Copy Number Variants in High-Risk Autism Families and Their Prevalence in a Large ASD Population di Matsunami, Nori, Hadley, Dexter, Hensel, Charles H., Christensen, G. Bryce, Kim, Cecilia, Frackelton, Edward, Thomas, Kelly, da Silva, Renata Pellegrino, Stevens, Jeff, Baird, Lisa, Otterud, Brith, Ho, Karen, Varvil, Tena, Leppert, Tami, Lambert, Christophe G., Leppert, Mark, Hakonarson, Hakon

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Genetic variation in CSF2 (5q31.1) is associated with longitudinal susceptibility to pediatric malaria, severe malarial anemia, and all-cause mortality in a high-burden malaria and... di Kisia, Lily E., Cheng, Qiuying, Raballah, Evans, Munde, Elly O., McMahon, Benjamin H., Hengartner, Nick W., Ong’echa, John M., Chelimo, Kiprotich, Lambert, Christophe G., Ouma, Collins, Kempaiah, Prakasha, Perkins, Douglas J., Schneider, Kristan A., Anyona, Samuel B.

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Bridging Islands of Information to Establish an Integrated Knowledge Base of Drugs and Health Outcomes of Interest di Boyce, Richard D., Ryan, Patrick B., Norén, G. Niklas, Schuemie, Martijn J., Reich, Christian, Duke, Jon, Tatonetti, Nicholas P., Trifirò, Gianluca, Harpaz, Rave, Overhage, J. Marc, Hartzema, Abraham G., Khayter, Mark, Voss, Erica A., Lambert, Christophe G., Huser, Vojtech, Dumontier, Michel

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Preferences of Information Dissemination on Treatment for Bipolar Disorder: Patient-Centered Focus Group Study di Kerner, Berit, Crisanti, Annette S, DeShaw, Jason L, Ho, Janika-Marie G, Jordan, Kimmie, Krall, Ronald L, Kuntz, Matt J, Mazurie, Aurélien J, Nestsiarovich, Anastasiya, Perkins, Douglas J, Schroeter, Quentin L, Smith, Alicia N, Tohen, Mauricio, Volesky, Emma, Zhu, Yiliang, Lambert, Christophe G

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